Tylototriton shanjing (Nussbaum, Brodie, & Yang, 1995) Mandarin Newt
(Tylototriton shanjing gallery)
Tylototriton shanjing
vs. Tylototriton verrucosus
Although often markedly different in appearance, Tylototriton shanjing
was formerly included in the species Tylototriton verrucosus, the
Himalayan Newt. In 1995, Ronald A. Nussbaum, Edmund D. Brodie, Jr., and
Yang Datong described T. shanjing as a separate species, based on
morphological characteristics. Prior to Nussbaum, Brodie, and Yang, 1995,
neither Anderson, who described T. verrucosus in 1871, nor
his predecessors made any mention of markedly different color
morphs, i.e. brightly colored as in T. shanjing, and uniform
dark as in the T. verrucosus holotype. This oversight has
been attributed to the type localities of the described specimens, which
indicate that either only bright colored, or only dark colored specimens
had been collected for study at any one time (Nussbaum, Brodie, Yang,
1995), making comparison impossible. Since Nussbaum, Brodie, and Yang,
1995, the bright colored morph has been described as a separate species based on
morphological and geological characteristics, and given the name Tylototriton shanjing,
which roughly translates to Mountain (shan) Demon/Spirit (jing) (Nussbaum,
Brodie, Yang, 1995). More specifically, all T. verrucosus
populations originally described from Yunnan province, China, with the exception
of a a small range in extreme western Yunnan, are considered T.
shanjing. The remaining range of T. verrucosus is large,
encompassing several countries and producing many probable
subspecies, and possibly one or more species. As the photos below
will demonstrate, differentiation of T. shanjing and T.
verrucosus based solely on "bright" or
"dark" coloration would be inaccurate, as the T.
verrucosus complex contains both bright and dark forms. In the future, we will
likely see changes within the T. verrucosus taxon.
T. shanjing have dark brown to black, semi-rough bodies with bright orange
heads, tails, dorsal ridges, legs, and feet. There are typically 6-14 orange
paratoid glands (concentrations of poison glands), often referred to as warts, on both sides of the slight dorsal
ridge that mark the rib peaks, and that make for a striking and unique appearance. The crown-like
cranial ridges, that have given
rise to the vernacular name Emperor Newt , are thought to be for
protection against predation. T. shanjing are a medium sized newt,
with adults attaining lengths up to 8 inches from snout to tail end.
Until recently, T. verrucosus had been described as uniform brown or
black, sometimes with faded orange-yellow coloration about the snout,
lower tail margin, and scattered about the belly, with an overall dark
appearance in comparison to T. shanjing. However, there are several
new types appearing in the pet trade that possess varying color schemes from
dark black, to moderate levels of orange, to high levels of orange that
appear similar to the bright colors characteristic of T. shanjing. Currently there are at least
three, probably more, distinct variations of the T. verrucosus complex appearing
in the pet trade, all of which lack description
and origin information. The main difference in these animals is coloration, however,
at least one type is smaller, with a distinct head, body, and tail shape.
Tables 1.1-1.2 show photos of T. shanjing and a few variations of the T.
verrucosus complex for physical comparison. Also note the highly
aquatic behavior of T. verrucosus compared to the more
terrestrial lifestyle of T. shanjing.
Today, we consider T.
shanjing and T. verrucosus to be allopatric, with T.
shanjing occurring in northern, western, and southwestern Yunnan
Province, and the T. verrucosus complex occupying extreme western Yunnan, extending
into Myanmar (Burma), India, Bhutan, Nepal, and possibly northern Vietnam.
Although their distributions are close at certain points, there is no
evidence of integration between the two species.
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Table 1.1: Typical
Tylototriton shanjing coloration and pattern. The photos
above show three typical T. shanjing, with vivid orange
heads, tails, dorsal ridges, legs, and dorsolateral paratoid
glands. Also note that with the exception of one, all of the
following photos of T. verrucosus are of aquatic
individuals; a characteristic not observed in T. shanjing
outside of breeding adults. T. shanjing are generally
differentiated from T. verrucosus by their more
terrestrial behavior, brighter orange coloration, usually in
higher levels, and narrower heads. Photos courtesy of Paolo
Mazzei,
Amphibians & Reptiles of Europe, and Jessica J. Miller. |
|
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Table 1.2: Variation
among members of the Tylototriton
verrucosus complex The photos above show
individuals of the T. verrucosus complex displaying a
wide range of coloration and shape, including high levels of
orange, moderate levels of orange, and high levels of black.
Also note the differences in tail and head shape. Whether the differences in
appearance between members of the T. verrucosus
complex warrant race or subspecies
classification is unknown at this time, but at least subspecies
classification seems likely. Photos courtesy of Henk
Wallays, Jessica J. Miller, and Dr. Grumman. |
Table 1.2 is included in the T. shanjing database entry to show
that at least one type of T. verrucosus are similar in appearance
to T. shanjing, which may shed some light on the possible reasons Anderson
and his predecessors might have overlooked the obvious differences between
the two species. As mentioned previously, it is assumed that the
differences between the two species were overlooked because only one type,
i.e. bright orange (shanjing) or dark (verrucosus), were
collected for study at any one time, making a morphological comparison
impossible (Nussbaum, Brodie, Yang, 1995). Also, if lighter colored specimens of the T. verrucosus
complex were compared to typical T. shanjing specimens, it's easy
to understand how and why they may have been included in the same species.
It is generally accepted that T.
shanjing will remain a separate species from T. verrucosus,
however, the new forms of T. verrucosus appearing in the pet trade
indicate there is more work to be done with this particular taxon.
Furthermore, some populations of T. shanjing differ markedly by tail
size, body length, and number of teeth, eluding to the feasibility of at
least one T.
shanjing subspecies (Nussbaum, Brodie, Yang, 1995).
Conservation Status
T. verrucosus, a species that
formerly included T. shanjing, has been classified as state major protective wildlife grade II
in China since 1988 (Zhao, 1998). Although T. shanjing was considered the same species as
T. verrucosus until
1995, it does not carry the same protection as T. verrucosus, and is basically unprotected
from over-collection and habitat destruction. The main threats to T. shanjing are human encroachment, habitat
destruction, and recently, over collection for the pet trade.
T. shanjing are highly sought after in the pet trade by
experienced keepers, as well as the less knowledgeable. During their
breeding season, T. shanjing are mass collected and shipped out to
other countries by the hundreds. By the time these newts make it to the
stores, they are often sick and close to death, and usually die shortly
after being purchased. Unfortunately, for the hundreds of newts collected
for trade, very few end up reproducing in captivity. The same can be said
for other Tylototriton species, including T. kweichowensis.
Hopefully, captive breeding successes will only increase, reducing or
eliminating the desire to purchase from pet stores, and in turn helping to
preserve wild populations.
Natural Habitat & Distribution
Tylototriton shanjing are found in the northern, central, western,
and southwestern Yunnan
Province, China, often near the Nu River (Nujiang), Lancang (Lancangjiang,
Mekong) River,
and Yuan River (Yuanjiang). The Nu and Lancang Rivers run from Tibet, southerly
through Yunnan Province. T. shanjing are found in
moist, vegetated areas, often close to ponds, irrigation canals, and rice
fields. T. shanjing do not usually enter bodies of water outside
of the breeding season, and remain hidden in dark places
during the day.
Documented populations are known to occur between
1000-2500 meters above sea level (Nussbaum, Brodie, Yang, 1995). This is not surprising, as Yunnan is
almost entirely mountainous. The map below-left shows the general
distribution of T. shanjing in the Yunnan Province of China. The map below-right shows
documented populations in Yunnan Province (adapted from Nussbaum, Brodie,
and Yang, 1995).


Yunnan is a highly diverse region, and home to more than half of
China's plant and animal species. The climate is varied, with glacial
and temperate zones in the northwest, mild to subtropical climates in
central and eastern areas, and hot, tropical climates in the south. T. shanjing are found
in temperate northwestern Yunnan, including the Lijiang Prefecture, the subtropical
western/central Yunnan, and even into down into the tropical southwestern
region. Of course, it's entirely possible that T. shanjing inhabits
only cooler microhabitats in the tropical zones, however, even such
environments would be significantly warmer than the colder areas of
northern Yunnan. Yunnan is approximately 94% highland, and 6%
flatlands, and so it is assumed that T. shanjing are found in
mostly, if not entirely, in mountainous regions. Yunnan also experiences two distinct seasons; dry,
and monsoon. In the Yunnan, the monsoon season begins lightly in May, with
the heaviest rains between June and September, and tapers off in October.
As Table 1.3 below shows, the monsoon season coincides with the warmer,
summer season, and that annual rainfall and temperatures vary greatly in
different regions of Yunnan.
| Table 1.3 -
Climates of selected Yunnan Prefectures, China, over the
past 20 years. Blue text indicates monsoon months. |
| |
 |
Lijiang
Prefecture |
|
| month |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
| avg temp. °F |
42.8 |
46.4 |
50.0 |
55.4 |
62.6 |
64.4 |
64.4 |
62.6 |
60.8 |
55.4 |
48.2 |
42.8 |
| avg high °F |
57.2 |
59.0 |
64.4 |
68.0 |
73.4 |
73.6 |
73.6 |
73.6 |
71.6 |
68.0 |
62.6 |
57.2 |
| avg low °F |
30.2 |
35.6 |
41.0 |
46.4 |
51.8 |
57.2 |
59.0 |
57.2 |
53.6 |
48.2 |
37.4 |
32.0 |
| rainfall (inches) |
.0394 |
.236 |
.433 |
.827 |
2.32 |
7.09 |
9.37 |
8.66 |
5.63 |
2.76 |
.512 |
.157 |
|
|
|
| |
 |
Dali
Prefecture |
|
| month |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
| avg. temp. °F |
46.4 |
50.0 |
55.4 |
60.8 |
66.2 |
68.0 |
60.8 |
64.4 |
64.4 |
59.0 |
53.6 |
48.2 |
| avg high °F |
60.8 |
62.6 |
68.0 |
73.4 |
77.0 |
77.0 |
77.0 |
75.2 |
75.2 |
69.8 |
64.4 |
60.8 |
| avg low °F |
37.4 |
39.2 |
44.6 |
50.0 |
55.4 |
42.8 |
62.6 |
60.8 |
59.0 |
51.8 |
44.6 |
37.4 |
| rainfall (inches) |
.551 |
.866 |
1.30 |
.827 |
2.64 |
8.23 |
7.24 |
9.41 |
6.46 |
3.94 |
1.3 |
.591 |
|
|
|
| |
 |
Dehong
Prefecture |
|
| month |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
| avg temp. °F |
53.6 |
57.2 |
64.4 |
69.8 |
73.4 |
75.5 |
75.2 |
75.2 |
73.4 |
69.8 |
62.6 |
55.4 |
| avg high °F |
71.6 |
75.2 |
82.4 |
86.0 |
86.0 |
82.4 |
82.4 |
82.4 |
82.4 |
80.6 |
77.0 |
73.4 |
| avg low °F |
42.8 |
44.6 |
50.0 |
59.0 |
64.4 |
69.8 |
69.8 |
69.8 |
68.0 |
62.6 |
53.6 |
44.6 |
| rainfall (inches) |
.472 |
.709 |
.709 |
2.24 |
5.20 |
12.3 |
15.9 |
14.0 |
6.46 |
4.96 |
1.85 |
.709 |
|
|
|
| |
 |
Kunming
Prefecture |
|
| |
| month |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
| avg temp. °F |
46.4 |
48.2 |
53.6 |
60.8 |
66.2 |
66.4 |
68.0 |
66.2 |
62.6 |
59.0 |
51.8 |
46.4 |
| avg high °F |
59.0 |
62.6 |
69.8 |
75.2 |
77.0 |
75.2 |
75.2 |
75.2 |
73.4 |
68.0 |
64.4 |
59.0 |
| avg low °F |
33.8 |
37.4 |
42.8 |
48.2 |
57.2 |
60.8 |
62.2 |
60.8 |
51.8 |
51.8 |
44.6 |
37.4 |
| rainfall (inches) |
.512 |
.433 |
.630 |
1.06 |
3.74 |
7.01 |
8.70 |
8.35 |
3.58 |
3.58 |
1.61 |
.551 |
|
|
|
| |
 |
Xishuangbanna
Prefecture |
|
| |
| month |
1 |
2 |
3 |
4 |
5 |
6 |
7 |
8 |
9 |
10 |
11 |
12 |
| avg temp. °F |
60.8 |
64.4 |
69.8 |
75.2 |
78.8 |
78.8 |
77.0 |
77.0 |
75.2 |
73.4 |
64.4 |
60.8 |
| avg high °F |
77.0 |
82.4 |
89.6 |
91.4 |
91.4 |
87.8 |
86.0 |
86.0 |
87.8 |
84.2 |
84.2 |
75.2 |
| avg low °F |
51.8 |
51.8 |
55.4 |
62.6 |
69.8 |
71.6 |
71.6 |
71.6 |
69.8 |
66.2 |
60.8 |
53.6 |
| rainfall (inches) |
.709 |
.433 |
.787 |
2.01 |
5.24 |
7.32 |
8.50 |
9.69 |
5.39 |
3.90 |
2.01 |
1.02 |
|
|
T. shanjing in Captivity
T. shanjing is a passive, non-aggressive species. One to two adults
can be housed in no smaller than
a 15 gallon aquarium, but the larger the tank, the better. This
species is not tolerant of improper habitats, such as excessive moisture, insufficient
moisture, overcrowding, mixed
species tanks, undesirable food items, or lack of hiding places. Multiple
hiding spots should be provided to prevent the newts from piling on top of
one another in the same spot. If healthy, housed in the proper
habitat, and not exposed to stressful activities, T. shanjing are
long lived captives.
T. shanjing are typically shy and timid initially, hiding
in dark places for the entirety of the day and emerging at night to feed.
Well adjusted individuals may emerge during the day to feed, and accept
food from forceps. Because of their
rather delicate and unforgiving nature, T. shanjing
are not recommended for novices.
A terrestrial or large semi-aquatic setup is ideal for housing T.
shanjing. Soil substrate should consist of a rich mixture, with a
healthy colony of nitrifying bacteria. Sterile substrates can cause
problems with amphibians, especially new imports of the more delicate
species because they allow potentially harmful pathogens brought in on the
amphibians to flourish and take over the tank. See
article
0021 - Substrate Mixes for the Vivarium for information about proper
substrate mixtures.
A basic
setup would consist of 4-6 inches of moist soil, a few live plants, and several dark
hiding places. Live
terrestrial plants, such as Epiprenum and Philodendron,
should be included in the land area. Hiding places, such as small caves and
shelters made of rock, wood, terra cotta, or other
non-toxic materials are a necessity with T. shanjing. The soil must always be kept
moist, but not soaking wet or muddy. The winter season in Yunnan is cold
and dry, which may seem odd to westerners, but is normal in areas that
experience a wet and humid monsoon season in the summer. For this reason, terrestrial
T. shanjing actually prefer somewhat drier terrestrial conditions
compared to some other species. It is recommended to
keep one half of the terrestrial portion of the tank wetter than the other, so the newts can choose the level of humidity
they prefer. Drier hiding spots, such as stacked flat rocks or other
material, should also be included.
For
breeding purposes, a sloped-floor water area of about 6-8 inches maximum
can be included. The water area can be mildly
filtered with carbon and sponge, and must be cycled prior to use with the newts (See
article
0009 - Introduction to the Nitrogen Cycle for more information about
cycling aquariums).
Live, aquatic plants should be included in the breeding area for egg
deposition, as well. Outside
of the breeding season, the water area should be drained or reduced to
only an inch or two; as mentioned previously, the non-breeding winter
season in Yunnan is colder and drier than the wet summer breeding season. This will aid in stimulating seasonal changes, for
during the breeding season, the water area can be flooded to simulate
rising water levels that would be experienced during the monsoon season in
Yunnan, when T. shanjing enters breeding mode. A water bowl is not
necessary with T. shanjing, as this species does not usually enter bodies of water outside the breeding
season. In fact, shallow, stagnant water areas, such as soaking bowls, can
provide a potential breeding ground for some harmful bacteria. Some may
prefer to transfer their newts into a larger aquarium during the breeding
season, in a similar fashion as many Triturus species.
Temperatures for T. shanjing are a somewhat controversial topic.
Although some recommend keeping T. shanjing in the upper-70's during the warmest season of the year, an acceptable range is
low to mid 70's during the warm months, and low to mid 60's during the winter months.
Temperatures in Yunnan are more extreme than these, but such a range is
not necessary in captivity, especially since T. shanjing has been
bred by maintaining the fore mentioned temperature scale. As table 1.3 shows, the monsoon
season is generally between May and October, which also corresponds to
warmer temperatures. Table 1.3 shows that the climate in Lijiang, northern
Yunnan, is considerably colder than that of Xishuangbanna, in southern
Yunnan, which indicates that populations of T. shanjing are found
in variable climates. It can be deduced that individuals from tropical
southern Yunnan are exposed to higher temperatures year-round, even if
populations exist only in cooler microhabitats, while those
those from colder northern populations may not be exposed to such high
temperatures. Further assumptions lead to the conclusion that those from
tropical southern Yunnan prefer higher temperatures for breeding purposes,
whereas those further north may actually enter dormancy in the wild. Unfortunately, it is usually impossible to know exactly where a
wild caught individual originated from, and so the fore mentioned temperatures
should be treated as "safety zone" temperatures that can be applied
to any individual.
As with all amphibians, tap water should be treated with a water
conditioner or primer prior to the introduction of inhabitants. Never use plain
tap water, de-ionized, distilled, or reverse osmosis water alone with amphibians.
See
article
0006 - Water Quality and Amphibians for more information about
water quality. See
article
0020 - Captive Habitats: Ideas, Instructions, and Examples and the
Captive
& Wild Habitats section of the
Photo
Gallery. See
article
0021 - Substrate Mixes for the Vivarium for information about proper
substrate mixtures.
Sexing & Breeding T. shanjing
Sexual dimorphism is limited in T. shanjing. In general, females can be distinguished from males by their larger, more robust
size. During the breeding season, males will develop swollen cloaca, and laterally
compressed tails.
In the wild, the breeding season occurs from May to August, which corresponds to
the monsoon season in their distribution in Yunnan. Courtship may consist of the
male and female turning in circles, underwater, with their snouts nearly
touching. Females will lay
their eggs singly, or in strings attached to submersed plants, rocks, or other materials. Some
have also reported eggs being deposited on moist land.
It is presumed that
most captive individuals, at least in the US and Europe, are likely from
the warmer southern regions of Yunnan that are less mountainous and closer to
surrounding countries, while newts from the higher elevation
populations of northern Yunnan are probably not collected for trade often.
At least a few breeders have reported success after a winter
at temperatures in the low to mid 60's, followed by a more humid and warmer
period with temperatures in the low to mid 70's. To stimulate breeding in captivity, it may be
beneficial to keep the water level lower or empty during the winter season, and
flood it during the warmer season. This may simulate the monsoon/breeding
season, and the drier, colder winter season of Yunnan to a degree, hopefully
enough to convince T. shanjing to enter breeding mode. Most newt
species will breed in captivity when kept in considerably less severe seasonal
changes than would be experienced in the wild, provided noticeable winter and
summer seasons in the proper humidity levels are supplied.
Larvae and new morphs should be kept in the low to mid 70's, preferably not below 69°F. These higher temperatures
correspond to the warmer temperatures experienced during summer in the wild.
Sustained lower temperatures may prove fatal to larvae and new morphs.
At least a few successful breeders of T. shanjing noted that the breeding adults were
long term, established captives housed in a moderately spacious tank. The establishment
of a small colony, or at least one healthy male-female pair is probably a crucial factor for breeding this species in
captivity, especially considering that most imported newts are unhealthy and do
not live long. Again, populations of T. shanjing are found in variable
climates, and it can be assumed that T. shanjing's affinity to breed
depends heavily on the environmental conditions of their natural habitat, as is
the case with most species. In
general, individuals from tropical southern Yunnan are probably exposed to
higher temperatures year-round, while those from colder northern
populations may not tolerate temperatures as high. The lack knowledge of climate preference
for captive individuals may be a key reason T. shanjing is so
difficult to breed in captivity, in addition to the difficulties of attaining healthy individuals.
Fortunately, the breeding habits of T.
shanjing are at least a little more known today, and captive breeding successes
are slowly increasing. There have been a few successful breeding projects in
zoos, and by dedicated enthusiasts in recent times. Hopefully, in the near
future T. shanjing will be bred in captivity often, and will become
abundant in the caudate community. It seems that the more common a species, the
less desirable it becomes, which can reduce its appeal to buyers, and thus to
collectors as well. In theory, as a species becomes less sought after, it is
collected less often from the wild, and thus wild populations may be positively
impacted by such captive breeding successes.
Journal References
Nussbaum, R. A., E. D. Brodie, Jr., and Y. Datong. 1995. A Taxonomic Review
of Tylototriton verrucosus Anderson (Amphibia: Caudata: Salamandridae).
Herpetologica 51(3): 257-268.
Chatterjee, K., and A. Majhl. 1974. Karotype of the Himalayan newt,
Tylototriton verrucosus. Norw. Journal of Zoology. 22: 65-66.
Printed Book References
Datong, Yang. The Amphibia-fauna of Yunnan.
China Forestry Publishing House, Beijing, 1991.
Zhao, E. China Red Data Book of Endangered Animals: Amphibia and
Reptilia.
Beijing, China: Science Press; Endangered Species Scientific Commission,
P.R.C.,
1998.
Zhao, E., et al. Studies on Chinese Salamanders.
Society for the Study of Amphibians and Reptiles, 1988.
Internet References
(1998). Yunnan Climates; A brief table of climates in some areas of Yunnan. Yunnan Travel.
http://www.sinohost.com/yunnan_travel/travel_info/yunnan_climate.html
(Accessed: 2003).
Mahoney, Meridith, and Vance Vredenburg. (1999). Tylototriton shanjing,
Emperor Newt. Amphibiaweb.
http://amphibiaweb.org/cgi-bin/amphib_query?rel-genus=like&upper-genus...etc. (Accessed: 2000).
Staniszewski, Marc S. (1998) Mandarin Salamander FAQ.
http://www.amphibian.co.uk/mandarin.html
(Accessed: 2000).
Yunnan Province. asinah.net.
http://www.asinah.net/chinaprovinces_yunan.html
(Accessed: 2000).
Additional Resources
AmphibiaWeb (Tylototriton shanjing entry)
Marc Staniszewski's Mandarin Salamander FAQ
Rieo.net (Tylototriton shanjing photos)
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